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Intracellular nucleosomes constrain a DNA linking number difference of ?1.26 that reconciles the Lk paradox

机译:细胞内核小体限制了DNA连接数差异的1.26,这使Lk悖论协调一致

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The interplay between chromatin structure and DNA topology is a fundamental, yet elusive, regulator of genome activities. A paradigmatic case is the “linking number paradox” of nucleosomal DNA, which refers to the incongruence between the near two left-handed superhelical turns of DNA around the histone octamer and the DNA linking number difference (?Lk) stabilized by individual nucleosomes, which has been experimentally estimated to be about ?1.0. Here, we analyze the DNA topology of a library of mononucleosomes inserted into small circular minichromosomes to determine the average ?Lk restrained by individual nucleosomes in vivo. Our results indicate that most nucleosomes stabilize about ?1.26 units of ?Lk. This value balances the twist (?Tw ≈?+?0.2) and writhe (?Wr?≈??1.5) deformations of nucleosomal DNA in terms of the equation ?Lk?=??Tw?+??Wr. Our finding reconciles the existing discrepancy between theoretical and observed measurement of the ΔLk constrained by nucleosomes.
机译:染色质结构和DNA拓扑之间的相互作用是基因组活动的基本但难以捉摸的调节剂。一个典型的例子是核小体DNA的“连接数悖论”,它是指在组蛋白八聚体周围的两个左手超螺旋DNA左旋和由单个核小体稳定的DNA连接数差(ΔLk)之间的不一致。在实验上已经估计约为1.0。在这里,我们分析了插入小的圆形微型染色体中的单核小体文库的DNA拓扑,以确定体内单个核小体抑制的平均ΔLk。我们的结果表明,大多数核小体稳定了约1.26个单位的LKk。该值根据等式ΔLk=ΔTwΔ+ΔWr平衡了核小体DNA的扭曲变形(ΔTw≈α+Δ0.2)和扭曲(ΔWr≈≈1.5)。我们的发现使核小体约束的ΔLk的理论测量值与观察到的测量值之间的现有差异得以调和。

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